Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 25
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 23
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 12
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 10
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 10
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7